» Articles » PMID: 21903238

NDMA Formation Kinetics from Three Pharmaceuticals in Four Water Matrices

Overview
Journal Water Res
Date 2011 Sep 10
PMID 21903238
Citations 4
Authors
Affiliations
Soon will be listed here.
Abstract

N, N-nitrosodimethylamine (NDMA) is an emerging disinfection by-product (DBP) that has been widely detected in many drinking water systems and commonly associated with the chloramine disinfection process. Some amine-based pharmaceuticals have been demonstrated to form NDMA during chloramination, but studies regarding the reaction kinetics are largely lacking. This study investigates the NDMA formation kinetics from ranitidine, chlorphenamine, and doxylamine under practical chloramine disinfection conditions. The formation profile was monitored in both lab-grade water and real water matrices, and a statistical model is proposed to describe and predict the NDMA formation from selected pharmaceuticals in various water matrices. The results indicate the significant impact of water matrix components and reaction time on the NDMA formation from selected pharmaceuticals, and provide fresh insights on the estimation of ultimate NDMA formation potential from pharmaceutical precursors.

Citing Articles

Biodegradation of Doxylamine From Wastewater by a Green Microalga, .

Xiong J, Cui P, Ru S Front Microbiol. 2020; 11:584020.

PMID: 33224120 PMC: 7669909. DOI: 10.3389/fmicb.2020.584020.


Removal of chlorpheniramine and variations of nitrosamine formation potentials in municipal wastewaters by adsorption onto the GO-FeO.

Lin C, Li C, Chen C, Chen W Environ Sci Pollut Res Int. 2019; 26(20):20701-20711.

PMID: 31102232 DOI: 10.1007/s11356-019-05278-9.


Reduction of N-nitrosodimethylamine formation from ranitidine by ozonation preceding chloramination: influencing factors and mechanisms.

Zou R, Liao X, Zhao L, Yuan B Environ Sci Pollut Res Int. 2018; 25(14):13489-13498.

PMID: 29492817 DOI: 10.1007/s11356-018-1470-z.


Formation mechanism of NDMA from ranitidine, trimethylamine, and other tertiary amines during chloramination: a computational study.

Liu Y, Selbes M, Zeng C, Zhong R, Karanfil T Environ Sci Technol. 2014; 48(15):8653-63.

PMID: 24968236 PMC: 4123930. DOI: 10.1021/es500997e.